Galactosemia
An autosomal recessive inherited metabolic disorder caused by mutations in the GALE, GALK1, and GALT genes. It is characterized by deficiency of the enzymes responsible for the metabolism of galactose. Signs and symptoms include intellectual disability, hepatomegaly, hepatic failure, and renal failure.
National Institute of Medical Science
Md Paediatrics
National Institute of Medical Science
MD pediatrics
Self Emploid(private Clinic)
Morbi
Shri M P Shah Medical College Jamnagar
M B B S
Super Specialist in Reproductive Endocrinology
Sanjay Gandhi Postgraduate Institute of Medical Sciences
Senior Resident
Sanjay Gandhi Postgraduate Institute of Medical Sciences
PDCC Paediatric Gastroenterology & Hepatology
Private Practise
Md
GRH Madurai
Mbbs
Madurai Medical College
MBBS
LLRM
Senior Resident
Dhanvantri Children Hospital
Consultant
Mrmc
MBBS,,,DCH
General Hospital Kanakapur
Md Pediatrics
MD Pediatrics
pediatrics
Dr Baba Sahib Ambedkar Medical College and Hospital
Ug Student